For researchers
Is your paper here?
2,673 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
25 matches for
Styrkarsdottir U,
showing the first 5.
New sequence variants associated with bone mineral density
Styrkarsdottir U,
Halldorsson BV,
Gretarsdottir S,
Gudbjartsson DF,
Walters GB,
Ingvarsson T,
Jonsdottir T,
Saemundsdottir J,
Snorradóttir S,
Center JR,
Nguyen TV,
Alexandersen P
and 7 more — show all
Nature genetics · 2009 · PMID 19079262
1 page
A variant in MCF2L is associated with osteoarthritis
Day-Williams AG,
Southam L,
Panoutsopoulou K,
Rayner NW,
Esko T,
Estrada K,
Helgadottir HT,
Hofman A,
Ingvarsson T,
Jonsson H,
Keis A,
Kerkhof HJ
and 33 more — show all
Thorleifsson G,
Arden NK,
Carr A,
Chapman K,
Deloukas P,
Loughlin J,
McCaskie A,
Ollier WE,
Ralston SH,
Spector TD,
Wallis GA,
Wilkinson JM,
Aslam N,
Birell F,
Carluke I,
Joseph J,
Rai A,
Reed M,
Walker K,
Doherty SA,
Jonsdottir I,
Maciewicz RA,
Muir KR,
Metspalu A,
Rivadeneira F,
Stefansson K,
Styrkarsdottir U,
Uitterlinden AG,
van Meurs JB,
Zhang W,
Valdes AM,
Doherty M,
Zeggini E
arcOGEN Consortium
American journal of human genetics · 2011 · PMID 21871595
1 page
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy
Bjornsdottir G,
Ivarsdottir EV,
Bjarnadottir K,
Benonisdottir S,
Gylfadottir SS,
Arnadottir GA,
Benediktsson R,
Halldorsson GH,
Helgadottir A,
Jonasdottir A,
Jonasdottir A,
Jonsdottir I
and 21 more — show all
Kristinsdottir AM,
Magnusson OT,
Masson G,
Melsted P,
Rafnar T,
Sigurdsson A,
Sigurdsson G,
Skuladottir A,
Steinthorsdottir V,
Styrkarsdottir U,
Thorgeirsson G,
Thorleifsson G,
Vikingsson A,
Gudbjartsson DF,
Holm H,
Stefansson H,
Thorsteinsdottir U,
Norddahl GL,
Sulem P,
Thorgeirsson TE,
Stefansson K
Nature communications · 2019 · PMID 30992453 · open access
1 page
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis gene
Boer CG,
Yau MS,
Rice SJ,
Coutinho de Almeida R,
Cheung K,
Styrkarsdottir U,
Southam L,
Broer L,
Wilkinson JM,
Uitterlinden AG,
Zeggini E,
Felson D
and 5 more — show all
Annals of the rheumatic diseases · 2021 · PMID 33055079 · open access
1 page
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk
Surakka I,
Fritsche LG,
Zhou W,
Backman J,
Kosmicki JA,
Lu H,
Brumpton B,
Nielsen JB,
Gabrielsen ME,
Skogholt AH,
Wolford B,
Graham SE
and 14 more — show all
Chen YE,
Lee S,
Kang HM,
Langhammer A,
Forsmo S,
Åsvold BO,
Styrkarsdottir U,
Holm H,
Gudbjartsson D,
Stefansson K,
Baras A,
Abecasis GR,
Hveem K,
Willer CJ
Regeneron Genetics Center
Nature communications · 2020 · PMID 33097703 · open access
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.